Spin castable resist composition and use

ABSTRACT

Spin castable polymethylmethacrylate photoresist compositions are provided utilizing certain cinnamic acid derivatives as dyes capable of absorbing light at about 436 nm and substantially transparent to light at about 220-250 nm. The spin castable polymethylmethacrylate resist compositions are used in making semiconductor devices by multilayer photoresist methods.

This application is a division of application Ser. No. 619,526 filedJune 11, 1984, U.S. Pat. No. 4,535,053.

BACKGROUND OF THE INVENTION

Prior to the present invention, as shown by Chen et al, U.S. Pat. No.4,362,809, for Multilayer Photoresist Process Utilizing an AbsorbantDye, polymethylmethacrylate (PMMA) photoresist compositions containingcoumarin as an absorbant dye, were used as a photoresist for etchingsemiconductor devices. Although the coumarin containing PMMAcompositions of Chen et al were found useful in the practice ofmultilayer photoresist methods using an upper portable conformable mask(PCM), coumarin was found to interfere with the delineation of the lowerPMMA resist layer during its subsequent UV exposure in the range ofabout 220-250 nm. As a result, an increase in the duration ofultraviolet light exposure time of the PMMA layer by a factor of atleast two was found necessary to overcome the coumarin absorption in theregion of 220-250 nm.

It would be desirable, therefore, to provide a PMMA photoresistcomposition having an absorbant dye which performed satisfactorily in amultilayer photoresist process using a portable conformable mask. Inorder to perform satisfactorily, the dye would have to be soluble in thePMMA and sufficiently non-volatile so that it could survive the initialspin and baking steps during the application of the PMMA on thesubstrate surface. The dye also would have to absorb at about 436 nmduring the initial exposure of the upper positive resist layer to effectthe formation of the PCM, which would substantially minimize unwantedreflections from the PMMA resist-substrate interface during such UVexposure. An additional criterion of the absorbant dye is that the dyewould have to be substantially non-absorbing in the range of about220-250 nm which would permit the delineation of the PMMA layer by adeep UV blanket through the PCM.

The present invention is based on the discovery that the certainderivatives of cinnamic acid having the formula ##STR1## where R and R¹are selected from hydrogen or C.sub.(1-8) alkyl, Q is --O-- or --N--, Xis selected from halogen and nitrile, R² is a monovalent group selectedfrom ##STR2## polyalkylene glycol, polyalkylene amide and polyalkyleneester and R³ is a C.sub.(1-8) alkylene radical or C.sub.(6-13) arylradical, have been found to be absorbant at about 400-465 nm,substantially transparent in the range of about 220-250 nm, soluble inan organic solvent solution of PMMA and in PMMA after spin casting andbaking.

BRIEF DESCRIPTION OF THE DRAWING

There is shown in the figure, the extinction coefficients of the1,3-propanediol diester of methyl(p-diethylamino-α-cyano)cinnamic acidand coumarin. These spectra were measured with a Perkin Elmer 330 UVSpectrophotometer in an ethanol solution.

The cinnamic acid derivatives of formula (I) which preferably can have amolecular weight in the range of about 350 to about 1000 are alsosubstantially non-volatile at temperatures in the range of about 100° C.to 200° C. As a result, spin castable PMMA compositions are providedwhich are capable of absorbing in the 436 nm region while substantiallytransparent in the 220-250 nm region. As a result, these photoresistscan be advantageously utilized in multilayer photoresists processeswithout the disadvantages of the prior art requiring excessive exposuretime due to a high level of absorbance in the 220-250 nm region.

STATEMENT OF THE INVENTION

There is provided by the present invention a spin castable photoresistcomposition comprising

(A) 100 parts of an inert organic solvent

(B) 1 to 15 parts of a polymethylmethacrylate and

(C) 0,01 to 1.0 parts of the cinnamic acid derivative of formula (I).

There is also provided by the present invention a process forphotopatterning a polymethylmethacrylate resist on a silicon substratewhich comprises

(1) spin casting onto a silicon substrate, a polymethylmethacrylateresin composition comprising

(A) 100 parts of an inert organic solvent

(B) 1 to 15 parts of a polymethylmethacrylate and

(C)0.01 to 1.0 parts of the cinnamic acid derivative of formula (I),

(2) baking the applied resist composition of (1) to a temperature of140° to 200° C. to produce a polymethylmethacrylate resist layer havinga thickness of from 1 to 3 microns,

(3) applying onto the layer of (2) a polynovolak resist to a thicknessof from about 0.2 to 1.0 microns,

(4) baking the resist layer of (3) to a temperature of about 70° to 110°C.,

(5) exposing the upper resist layer of (4) to patterned UV light atabout 350 to 440 nm to produce a latent positive image in the resist,

(6) developing the resist of (5) and thereafter baking the resultingportable conformable mask,

(7) exposing the composite of the resulting portable conformable maskand the polymethylmethacrylate resist layer to UV light in the range of190 to 250 nm to produce a positive image of the portable conformablemask, and

(8) developing the resulting polymethylmethacrylate resist.

There are included by the cinnamic acid derivatives of formula (I)compounds such as ##STR3##

Polymethylmethacrylate resists which can be utilized in the practice ofthe present invention are, for example, Elvacite® 2041 and 2010, of theDupont de Nemours Company, Wilmington, Del.; KT1 Standard PMMA resists,etc.

The lower average molecular weight of PMMA 2010 permits a 2 micron filmthickness in a single spin coating application. Additionalcharacteristics of PMMA 2010 and PMMA 2041 are shown in the followingtable

    ______________________________________                                                       PMMA 2010 PMMA 2041                                            ______________________________________                                        Avg. molecular weight                                                                          150,000     500,000                                          Max. Thickness per spinning                                                                    2 μm     1 μm                                          Range of r/r.sub.o in MIBK                                                                     20-120      20-200                                           in chlorobenzene 20-80       30-120                                           in toluene       20-120      20-200                                           r.sub.o in MIBK (nm/min)                                                                       56          14                                               r.sub.o in chlorobenzene                                                                       381         63                                               r.sub.o in toluene                                                                             73          29                                               ______________________________________                                    

Among the positive photoresist compositions which can be used in theproduction of the PCM (portable conformable mask), there are includednovolak resins modified with naphthoquinonediazides as shown in thechemical behavior of positive working systems by Jeffrey C. Streeter,Eastman Kodak Company, Proceedings of the Microelectronic SeminarInterface '76, pp. 116-121. A typical reaction for preparing thesepositive photoresists is to react the hydroxyl groups on aphenol-formaldehyde resin with naphthoquinonediazide sulfonyl chloride.The most common solvents used in the novolak positive resists are2-ethoxyethylacetate and 2-methoxyethylacetate. In some cases, xyleneand butylacetate can be incorporated into the solvent system to givevarious drying and coating characteristics.

In the practice of the invention, a the PMMA photoresist composition canbe made by blending together commercially available PMMA which can havea molecular weight in the range of from about 100,000 to 900,000 with anorganic solvent such as chlorobenzene, toluene, etc., and the cinnamicacid derivative as shown in formula (I). The resulting PMMA compositionsare spin castable.

In the practice of the method of the present invention, the PMMAcomposition containing the cinnamic acid derivative can be spun onto asilicon wafer to a thickness of about 1.7 microns. Depending upon themolecular weight of the PMMA, the spinning of the PMMA composition canbe accomplished in several steps or in a single spin coatingapplication. If desired, the applied PMMA coating can be baked duringmultiple applications or it can be baked to a temperature in the rangeof about 140° to 200° C. for 30 minutes if in a final bake.

The top positive novolak resist layer is then spun onto the PMMAsurface. After a thickness of 0.5 microns is achieved with the topnovolak resist it is baked at a temperature in the range of 70° to 90°C. for a period of 1 to 30 minutes. The novolak resist is then exposedto ultraviolet employing a Mercury Arc lamp having an intensity of 100mW/cm² and a wave length of from 360 to 440 nm for a period of from 0.3to 1 seconds.

Experience has shown that a soak in a NaOH solution can provide foradvantageous results in the applied novolak resist prior to exposure.The NaOH should have a molar concentration in the range of 0.2 to 0.5for optimum results. If desired, the developed PCM can then be oxygenplasma cleaned in accordance with the procedure of Petrillo et al,Submicrometer Contact Hole Delineation with a Two-Layer Deep-UV PortableConformable Masking System, J. Vac. Sci. Technol. B 1(4), Oct.-Dec.1983. The positive resist PMMA composite can be exposed to UVirradiation having a wave length of from 190 to 250 nm. The resultingexposed PMMA composite can then be developed utilizing a standardacetone/isopropanol solution to produce a submicrometer contact hole toproduce a multilayer photoresist having a patterned PMMA photoresistlayer on a silicon wafer useful for making a semiconductor device.

In order that those skilled in the art will be better able to practicethe invention, the following example is given by way of illustration andnot by way of limitation. All parts are by weight.

EXAMPLE

A mixture of p-diethylaminobenzaldehyde (24.2 g, 0.136 mole) methylcyanoacetate (13.5 g, 0.136 mole), ε-aminocaproic acid (0.33 g) andglacial acetic acid (3 ml) in 40 ml of toluene was refluxed in a flaskequipped with a Dean-Stark trap and a condensor. After about 2 hours thetheoretical quantity of water (2.4 ml) was collected. The hot solutionwas treated with activated charcoal and filtered through Celite. Thetoluene was removed under reduced pressure and replaced with 95%ethanol. On cooling 30.4 g (0.118 mole, 86.5% yield) ofmethyl(p-diethylamino-α-cyano)-cinnamate orange needles were depositedand collected: mp 87°-89° C.

A 250 ml flask was charged with 19.1 g (0.074 mole) of themethyl(p-diethylamino-α-cyano)cinnamate, 2.84 g (0.0373 mole) ofdistilled 1,3-propanediol, 0.1 g of sodium hydride and 60 ml of dimethylsulfoxide (distilled from calcium hydride). The mixture was stirred andheated at 100°-110° C. at a pressure of about 30 torr for 5 hours. Thetemperature was then raised to distill off the dimethyl sulfoxide. Theremaining dark red material was crystallized from 95% ethanol, affording14.1 g of the crude dimer, mp 110° C. Further recrystallization gave10.6g (0.02 mole, 54% yield) of crystalline 1,3-propanediol diester ofp-diethylamino-α-cyano cinnamic acid having a melting point of 136°-138°C.

There was added to 33 g of a 6% by weight solution of Elvacite 2041 inchlorobenzene, 0.1 g of the cinnamyl ester. The mixture was stirred forone half hour, then filtered through a 0.2μ Teflon® resin membranefilter.

The chlorobenzene solution of PMMA and the cinnamyl ester was pouredonto silicon wafers and spun at 4000 rpm for 24 seconds. The resultingfilm was washed in a convection oven at 190° C. for 30 min. Another filmwas likewise coated onto the first layer and again baked for 30 min. Athird layer was then coated and baked to give a total thickness of about1.7μ. The dyed PMMA film was then coated with Shipley AZ-1450B to athickness of 0.5μ using a Macronetics photoresist coater equipped with atrack oven set at 87° C. The top photoresist layer was printed using anOptimetrix stepper. The top layer resist was then spray developed withShipley AZ-351 developer diluted 1 part with 3 parts water. Exposure ofthe PMMA layer was accomplished by flood illumination using a FusionSystems Microlite lOOC equipped with a mercury bulb. An exposure of 95seconds at 40 mW/cm² was used. The wafer was subsequently spraydeveloped using diglyme for 24 seconds, followed by an isopropanolrinse. Based on this procedure, there was obtained a patternedphotoresist having isolated 0.8μ lines and spaces over 0.5μ SiO₂ steps.

Although the above example is directed to only a few of the very manyvariables which can be utilized in the practice of the presentinvention, it should be understood that the present invention isdirected to a much broader variety of cinnamic acid derivatives as shownby formula (I) in combination with various polymethylmethacrylates andnovolak resins to produce a multilayer photoresist as shown in thedescription preceding this example.

What we claim as new and desire to secure by Letters Patent of theUnited States is:
 1. A spin castable photoresist compositioncomprising(A) 100 parts of an inert organic solvent (B) 1 to 15 parts ofa polymethylmethacrylate and (C) 0.01 to 1.0 part of a cinnamic acidderivative of the formula ##STR4## where R and R¹ are selected fromhydrogen or C.sub.(1-8) alkyl, Q is --O-- or --N--, X is selected fromhalogen and nitrile, R² is a monovalent group selected from ##STR5##polyalkylene glycol, polyalkylene amide and polyalkylene ester and R³ isa C.sub.(1-8) alkylene radical or C.sub.(6-13) aryl radical.
 2. A spincastable composition in accordance with claim 1, where the cinnamic acidderivative is 1,3-propanediol diester of p-diethylamino-α-cyano cinnamicacid.